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Perry Syndrome
Known as:
PARKINSONISM WITH ALVEOLAR HYPOVENTILATION AND MENTAL DEPRESSION
National Institutes of Health
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Related topics
Related topics
9 relations
Apathy
Autosomal dominant inheritance
Inappropriate behavior
Mental Depression
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Broader (1)
Hypoventilation
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2020
2020
Perry syndrome: a case of atypical parkinsonism with confirmed DCTN1 mutation.
E. McManus
,
G. Poke
,
M. Phillips
,
F. Asztely
The New Zealand medical journal
2020
Corpus ID: 216107900
Perry syndrome is a rare neurological condition characterised clinically by depression, sleep disturbance, central…
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2020
2020
Perry syndrome: a case of atypical parkinsonism with confirmed DCTN1 mutation: a response.
P. Tacik
,
Z. Wszolek
The New Zealand medical journal
2020
Corpus ID: 220653784
With great interest, we have read the article entitled “Perry syndrome: a case of atypical parkinsonism with confi rmed DCTN1…
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2019
2019
Neuropathological findings in a South Korean patient with Perry syndrome.
E. Chung
,
S. Kim
,
+4 authors
N. Cairns
Clinical Neuropathology
2019
Corpus ID: 209341875
OBJECTIVE The Korean patient with Perry syndrome (PS) was the first to come to autopsy. We report a pathologically confirmed…
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2019
2019
A case of Perry Syndrome responding to intestinal infusion of carbidopa/levodopa.
Moath Hamed
,
Aakash Shetty
,
G. Tremain
,
A. Lazarescu
,
O. Suchowersky
Parkinsonism & Related Disorders
2019
Corpus ID: 53109665
2018
2018
DCTN1 F52L mutation case of Perry syndrome with progressive supranuclear palsy-like tauopathy.
H. Honda
,
N. Sasagasako
,
+6 authors
T. Iwaki
Parkinsonism & Related Disorders
2018
Corpus ID: 3666089
2018
2018
Diaphragmatic Pacemaker for Perry Syndrome.
T. Konno
,
Z. Wszolek
Mayo Clinic proceedings
2018
Corpus ID: 46820431
2017
2017
Dysphagia in Perry Syndrome: Pharyngeal Pressure in Two Cases
G. Umemoto
,
Y. Tsuboi
,
+6 authors
M. Sakai
Case Reports in Neurology
2017
Corpus ID: 38864840
Background: To investigate the impact of dysphagia in Perry syndrome (PS), an autosomal dominant parkinsonism caused by mutation…
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2014
2014
p150glued-Associated Disorders Are Caused by Activation of Intrinsic Apoptotic Pathway
K. Ishikawa
,
S. Saiki
,
+8 authors
N. Hattori
PLoS ONE
2014
Corpus ID: 10322927
Mutations in p150glued cause hereditary motor neuropathy with vocal cord paralysis (HMN7B) and Perry syndrome (PS). Here we show…
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2009
2009
Christian Wider, MD — On Unraveling the Pathology of Perry Syndrome
E. Stump
2009
Corpus ID: 72238491
Swiss movement disorders neurologist Christian Wider, MD, hasn’t wasted time while in the US these past three years. Now…
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2008
2008
DCTN1 mutations in families with parkinsonism, depression, weight loss and central hypoventilation: Perry syndrome
M. Farrer
,
M. Hulihan
,
+17 authors
Z. Wszolek
2008
Corpus ID: 69072984
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